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rs121912503

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912503(C;T)
Make rs121912503(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position160650438
GeneLPA
is asnp
is mentioned by
dbSNPrs121912503
ebirs121912503
HLIrs121912503
Exacrs121912503
Varsomers121912503
Maprs121912503
PheGenIrs121912503
hapmaprs121912503
1000 genomesrs121912503
hgdprs121912503
ensemblrs121912503
gopubmedrs121912503
geneviewrs121912503
scholarrs121912503
googlers121912503
pharmgkbrs121912503
gwascentralrs121912503
openSNPrs121912503
23andMers121912503
23andMe allrs121912503
SNP Nexus

SNPshotrs121912503
SNPdbers121912503
MSV3drs121912503
GWAS Ctlgrs121912503
Max Magnitude0
OMIM152200
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121912503(A,T;A,T)
Alt rs121912503(A,T;A,T)
Reference rs121912503(C;C)
Significance Pathogenic
Disease Lipoprotein(a) deficiency
Variation info
Gene LPA
CLNDBN Lipoprotein(a) deficiency, congenital
Reversed 1
HGVS NC_000006.11:g.161071470G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015535.26,